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| Treatment of slight to moderately severe bleeding and prevention of bleeding in more minor procedures in mild haemophilia A and Von Willebrand’s disease |
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| Nocturnal enuresis |
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| Diabetes insipidus |
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| Diagnosis of diabetes insipidus |
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| Renal function test |
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No information available on dose adjustment in renal impairment.
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The complete list of all undesirable drug reactions can be found in the national Summary of Product Characteristics (SmPC) – click here
In children, in combination with ample fluid intake, very severe hyponatremia may develop, resulting in headache, abdominal pain, nausea, vomiting, weight gain, dizziness, confusion, malaise, memory impairment, vertigo, falling and in severe cases, convulsions and coma.
Oral use:
Common (> 1%): headache
Uncommon (0.1-1%): affect lability, aggression, abdominal pain, nausea, vomiting, diarrhea, peripheral edema, fatigue.
Rare (<0.1%): anxiety, nightmares, mood changes, drowsiness, hypertension, irritability.
Side effects of unknown frequency: anaphylactic reactions, hyponatremia, abnormal behavior, emotional disorders, depression, hallucinations, insomnia, attention deficit disorders, psychomotor hyperactivity, convulsions, nosebleeds, allergic dermatitis, rash, sweating, urticaria.
When used nasally, observed mainly in children and adolescents:
Very common (> 10%): increased body temperature.
Common (> 1%): sleep disorders, affect lability, nightmares, nervousness, aggression, upper respiratory tract infections
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The complete list of all contra-indications can be found in the national Summary of Product Characteristics (SmPC) – click here
No information available on specific contra indications in children.
The complete list of all warnings and precautions can be found in the national Summary of Product Characteristics (SmPC) – click here
In the treatment of enuresis nocturna and nycturia, fluid intake should be restricted as much as possible from 1 hour before administration at bedtime until the following morning, and in any case until at least 8 hours after administration. Treatment without concurrent restriction of fluid intake may result in fluid retention and/or hyponatremia with or without warning symptoms (headache, nausea/vomiting, weight gain and, in severe cases, convulsions and coma). Brain edema has been reported rarely in children and young adults treated with desmopressin acetate for enuresis nocturna.
All patients or, if appropriate, their caregiver, should be properly instructed to adhere to fluid restriction.
For the indication haemophilia A / vWD, desmopressin should only be administered intravenously due to the high doses in small children weighing less than 20 kg. Especially in these young children, be aware not only of tachycardia and flushing but also of the occurrence of water intoxication (hyperhydration); for 12 hours after using desmopressin there is a strict fluid restriction of 100 ml. This is the reason why many haemophilia treatment centres do not administer desmopressin to children younger than 3 years and in children between 3 and 6 years of age only with caution and under strict observation with regard to fluid intake and excretion (Pabinger 2015). Due to the risk of severe side effects (convulsions, coma due to hyponatraemia), when administering desmopressin to young children weighing < 20 kg, it is recommended that the effect should be to clinically monitored with checks of the serum sodium up to 24 hours after administration. Especially in young children or on repeated administration, be aware that hyponatraemia can occur due to the antidiuretic effect of desmopressin.
In concomitant use of drugs that disrupt the release of ADH, such as tricyclic antidepressants, SSRIs, chlorpromazine, loperamide and carbamazepine there is an increased risk of water intoxication. Hyponatraemia can also occur with concomitant use of NSAIDs.
The effect on clotting after desmopressin is administered varies greatly between individuals; intra-individually, the response is constant. It is recommended that a test dose should be given to determine the effect of administration on the factor VIII plasma concentration, VWF:RCo and VWG:Ag, thrombocyte count and, if necessary, PFA100, as well as to document tolerance in the individual patient (desmopressin test). Desmopressin is not effective in severe haemophilia A, all forms of haemophilia B and Von Willebrand’s disease type 3.
Only carry out the renal concentration test in infants when strictly indicated and in the clinic.
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The complete list of all interactions can be found in the national Summary of Product Characteristics (SmPC) – click here
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